Progressive Osseous Heteroplasia: A Rare Case Report

Progressive osseous heteroplasia (POH) is a rare genetic condition of progressive extraskeletal bone formation. POH is clinically suspected by cutaneous ossification, usually presenting in early life, that involves subcutaneous and then subsequently deep connective tissues, including muscle and fasc...

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Detalles Bibliográficos
Autores principales: Sahu, Kananbala, Rout, Arpita N., Mohapatra, Liza, Mohanty, Prasenjeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413444/
https://www.ncbi.nlm.nih.gov/pubmed/32832452
http://dx.doi.org/10.4103/idoj.IDOJ_502_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413444/
https://www.ncbi.nlm.nih.gov/pubmed/32832452
http://dx.doi.org/10.4103/idoj.IDOJ_502_19

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